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钆标记可生物降解的树突状-透明质酸杂化及其随后作为安全有效的磁共振成像造影剂的应用。

Gadolinium-Labeled Biodegradable Dendron-Hyaluronic Acid Hybrid and Its Subsequent Application as a Safe and Efficient Magnetic Resonance Imaging Contrast Agent.

机构信息

Huaxi MR Research Center (HMRRC), Department of Radiology, West China Hospital, Sichuan University , Chengdu, Sichuan 610041, China.

National Engineering Research Center for Biomaterials, Sichuan University , Chengdu 610064, China.

出版信息

ACS Appl Mater Interfaces. 2017 Jul 19;9(28):23508-23519. doi: 10.1021/acsami.7b06496. Epub 2017 Jul 10.

Abstract

Novel magnetic resonance imaging (MRI) contrast agents with high sensitivity and good biocompatibility are required for the diagnosis of cancer. Herein, we prepared and characterized the gadolinium [Gd(III)]-labeled peptide dendron-hyaluronic acid (HA) conjugate-based hybrid (dendronized-HA-DOTA-Gd) by combining the advantages of HA and the peptide dendron. The dendronized-HA-DOTA-Gd hybrid with 3.8% Gd(III) as weight percentage showed a negative zeta potential (-35 mV). The in vitro degradation results indicated that the dendronized-HA-DOTA-Gd hybrid degraded into products with low molecular weights in the presence of hyaluronidase. The dendronized-HA-DOTA-Gd hybrid showed a 3-fold increase in longitudinal relaxivity and much higher in vivo signal enhancement in 4T1 breast tumors of mice compared with clinical Magnevist (Gd-DTPA). The dendronized-HA-DOTA-Gd hybrid had a higher accumulation in tumors than Gd-DTPA; it was 2-3-fold after administration. Meanwhile, the polymeric hybrid resulted in low Gd(III) residue in the body compared with that of Gd-DTPA. The systematic biosafety evaluations, including blood compatibility and toxicity assessments, suggested that the dendronized-HA-DOTA-Gd hybrid exhibited good biocompatibility. Thus, the gadolinium-labeled and dendronized HA hybrid shows promise as a safe and efficient macromolecular MRI contrast agent based on high sensitivity, low residue content in the body, and good biosafety.

摘要

新型磁共振成像(MRI)对比剂需要具有高灵敏度和良好的生物相容性,以便用于癌症的诊断。在此,我们通过结合透明质酸(HA)和肽树枝状大分子的优势,制备并表征了基于钆[Gd(III)]标记的肽树枝状大分子-透明质酸(HA)偶联物的杂化体(树枝状大分子化-HA-DOTA-Gd)。树枝状大分子化-HA-DOTA-Gd 杂化物的重量百分比为 3.8%的 Gd(III),其具有负的 Zeta 电位(-35 mV)。体外降解结果表明,树枝状大分子化-HA-DOTA-Gd 杂化物在透明质酸酶存在的情况下降解为低分子量产物。与临床用 Magnevist(Gd-DTPA)相比,树枝状大分子化-HA-DOTA-Gd 杂化物的纵向弛豫率提高了 3 倍,在 4T1 乳腺癌小鼠的体内信号增强也更高。与 Gd-DTPA 相比,树枝状大分子化-HA-DOTA-Gd 杂化物在肿瘤中的积累更高;给药后是其 2-3 倍。同时,与 Gd-DTPA 相比,聚合物杂化物在体内导致的 Gd(III)残留量较低。包括血液相容性和毒性评估在内的系统生物安全性评价表明,树枝状大分子化-HA-DOTA-Gd 杂化物具有良好的生物相容性。因此,基于高灵敏度、体内残留量低和良好的生物安全性,标记了 Gd 的树枝状大分子化 HA 杂化物具有作为安全有效的大分子 MRI 对比剂的潜力。

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